跳至主要内容
临床试验/CTRI/2013/10/004071
CTRI/2013/10/004071已完成Unknown

A prospective, open-label, multicentre, non-comparative, post marketing observational study evaluating effectiveness and tolerability of Carbamazepine (TEgrital®) As Monotherapy in treatment naïve patients with generalized tonic-clonic seizures in routine clinical practice in India.

Novartis India Limited1 个研究点 分布在 1 个国家目标入组 493 人开始时间: 2013年1月18日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
493
试验地点
1
主要终点
•Change in number of seizure episode from baseline as response to Carbamazepine at 24 weeks.

研究概览

简要总结

Protocol synopsisxml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /

Title of study:

A prospective, open-label, multicentre, non-comparative, post marketing observational study evaluating effectiveness and tolerability of Carbamazepine (Tegrital®) as monotherapy in treatment naïve patients with generalized tonic-clonic seizures in routine clinical practice in India.

Purpose and rationale:

Epilepsy is the most common serious neurological disorder and is one of the world’s most prevalent non-communicable diseases. It is estimated that the condition affects approximately 50 million people, around 40 million of them living in developing countries1. The incidence of epilepsy in low-income countries may be as high as 190 per 100 000 people2. Consequently, in the context of the large and rapidly increasing populations in these countries, epilepsy is a significant health and socioeconomic burden requiring urgent attention3 4.

In 1990, the UK National General Practice Study of newly diagnosed epilepsy found that of 564 incident cases, 29% had primary and 28% secondary GTCS.5In 1993, Hauser et al. reporting on the Rochester study for the years 1935–1984 found that secondarily generalized seizures and GTCS constituted figures of 15 and 10, respectively, of their total age-adjusted incidence of 44 per 100,000 patient-years.6 Murthy et al. in a hospital-based cohort of 2531 patients, found that 162 (6.4%) had idiopathic generalized epilepsies (IGE), and 503 (19.9%) were unclassified.7 The SANAD A and B studies with a total of 2437 patients, 559 (23%) had either generalized (excluding childhood absence epilepsy) or unclassified seizures. 8

Sridharan et al. in 1999 projected number of people with epilepsy in India to be 5.5 million by the year 2001 and based on the incidence of epilepsy, the number of new cases of epilepsy each year to be close to half a million, the number of people with epilepsy in rural areas was projected to be around 4.1 million by the year 2001.9

Antiepileptic drugs (AEDs) are the mainstay of the treatment of epilepsy, and although their number has expanded exponentially, current principles governing drug therapy are in many ways similar to those established a century ago.10 Because AED therapy is typically maintained for several years and often for life, particularly in adults, a decision to initiate treatment has far-reaching consequences and needs to be based on careful risk-benefit analyses.11 12

Recently released NICE 2012 guidelines on the diagnosis and management of the epilepsies in adults and children in primary and secondary care have placed Carbamazepine as first-line treatment in children, young people and adults with newly diagnosed generalised tonic clonic seizures.13

Carbamazepine is a dibenzazepine derivative, its spectrum of activity embraces: partial seizures (simple and complex) with and without secondary generalization; generalized tonic-clonic seizures, as well as combinations of these types of seizures. Carbamazepine stabilizes hyperexcited nerve membranes, inhibits repetitive neuronal discharges, and reduces synaptic propagation of excitatory impulses. The prevention of repetitive firing of sodium-dependent action potentials in depolarized neurons via use- and voltage-dependent blockade of sodium channels may be its main mechanism of action. Whereas reduction of glutamate release and stabilization of neuronal membranes may account mainly for the antiepileptic effects, the depressant effect on dopamine and noradrenaline turnover could be responsible for the antimanic properties of carbamazepine

Carbamazepine is available as Tegrital® in India and is indicated for the treatment of partial seizures and generalized tonic-clonic seizures, in adults and in children. Although there is ample amount of clinical data highlighting the safety and efficacy of carbamazepine, but there is dearth of such data in the Indian scenario. This current study is designed to analyze the extended effectiveness and tolerability of Tegrital® (Carbamazepine) in treatment of children and adults with newly diagnosed generalized tonic-clonic seizures in Indian population.

研究设计

研究类型
Observational

入排标准

年龄范围
1.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Male and female out patients > 1 year to < 60 years of age with diagnosis of generalized tonic-clonic seizures that have been prescribed Carbamazepine as monotherapy (in OAED naïve patients) as per local prescribing information.
  • 2.Patients or their parent/legally-authorized guardian having given written, informed consent and/or assent to have their data collected after the nature of the trial had been fully explained (according to the local legal regulatory requirements).
  • Patients will not need to consent for taking the drug, as their treatment is decided before entry into the study and is part of their medical care.
  • 3.Patients who agree to follow medication as per local prescribing information of the study drug while participating in the study.

排除标准

  • Patients who meet any of the following criteria are not eligible for inclusion in this study: 1.Patients with absence seizure or with juvenile myoclonic seizure.
  • 2.Patients who require two or more anti-epileptic drug.
  • 3.Patients with any psychiatric coexistent illness that may affect the patient’s compliance with study procedures.
  • 4.Known hypersensitivity to the study drug, excipients or to drugs of similar chemical classes.
  • 5.Pregnant or nursing (lactating) women.
  • 6.Women of child-bearing potential (WOCBP), defined as all women physiologically capable of becoming pregnant, including women whose career, lifestyle, or sexual orientation precludes intercourse with a male partner and women whose partners have been sterilized by vasectomy or other means, UNLESS they are using two birth control methods.
  • The two methods can be a double barrier method (if accepted by local ethics committee) or a barrier method plus a hormonal method.
  • •Adequate barrier methods of contraception include: diaphragm, condom (by the partner), intrauterine device (copper or hormonal), sponge or spermicide.
  • Hormonal contraceptives include any marketed contraceptive agent that includes an estrogen and/or a progestational agent.
  • Reliable contraception should be maintained throughout the study and for 7 days after the study.
  • •Woman are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or six months of spontaneous amenorrhea with serum FSH levels 40 mIU/ml [for US only: and estradiol 20 pg/ml] or have had surgical bilateral oophorectomy (with or without hysterectomy) at least six weeks ago.
  • In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow-up hormone level assessment.
  • 7.Any other contra-indication according to local prescribing information for study drug.

结局指标

主要结局

•Change in number of seizure episode from baseline as response to Carbamazepine at 24 weeks.

时间窗: •Change in number of seizure episode from baseline as response to Carbamazepine at 24 weeks.

次要结局

  • •Percentage of patients experiencing (i) ≥50% reduction in number of seizures per month and (ii) ≥75% reduction in number of seizures per month after 24 weeks treatment.(•Physicians and subjects global evaluation of improvement in seizure severity & Physicians and subjects global evaluation of tolerability after 24 weeks treatment)

研究者

申办方类型
Pharmaceutical industry-Global

研究点 (1)

Loading locations...

相似试验